... currently seeking a Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross functionally with our clinical operations, medical and regulatory ... language Some clinical research experience is beneficial; and Working ...
... including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications ... is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, ...
... are knowledgeable about treatment guidelines, clinical research processes, and EU pharma regulations ...
... . As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, ... as an Intern In-house Clinical Research Associate or Intern Start-up ...
... are knowledgeable about treatment guidelines, clinical research processes, and EU pharma regulations ...
... are knowledgeable about treatment guidelines, clinical research processes, and EU pharma regulations ...
... to shape the future of clinical development. As a Clinical Research Associate II at ICON, you’ll ...
... global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology ...
... development, from pre-clinical research to regulatory submissions (MAA, NDA ... BLA). Key Responsibilities: Offer strategic regulatory advice and support to project teams. Oversee all clinical development aspects ...
... the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ... : tracks progress of the clinical trial, manages study data, budget, ... -2 years of relevant clinical trial experience with associated skill ...